Depuy Synthes Spine
FDA adverse event reports naming Depuy Synthes Spine as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: DEPUY SYNTHES SPINE.
- Total reports
- 4,728
- Deaths
- 32
- Injuries
- 1,911
- Malfunctions
- 2,782
Reports per year
1512
59013
1,07114
1,08015
94616
90617
11918
119
Source: FDA adverse event reports by year received, 2012–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Thoracolumbosacral Pedicle Screw SystemNKB1,811
- ScrewdriverHXX570
- Driver, ProsthesisHWR552
- Orthopedic Manual Surgical InstrumentLXH343
- Spinal Vertebral Body Replacement DeviceMQP198
- Appliance, Fixation, Spinal Intervertebral BodyKWQ195
- Cement, Bone, VertebroplastyNDN187
- Appliance, Fixation, Spinal InterlaminalKWP159
- Orthosis, Spinal Pedicle FixationMNI137
- ProbeHXB53
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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